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MODEL 253-11 CYBERLITH PULSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K800895
510(k) Type
Traditional
Applicant
INTERMEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/24/1980
Days to Decision
3 days

MODEL 253-11 CYBERLITH PULSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K800895
510(k) Type
Traditional
Applicant
INTERMEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/24/1980
Days to Decision
3 days